首页 | 本学科首页   官方微博 | 高级检索  
检索        

apelin-13下调caveolae可促进血管平滑肌细胞增殖
引用本文:毛小环,李兰芳,高晶,杨莉,柳威,秦旭平,陈临溪.apelin-13下调caveolae可促进血管平滑肌细胞增殖[J].中国临床康复,2011(46):8603-8608.
作者姓名:毛小环  李兰芳  高晶  杨莉  柳威  秦旭平  陈临溪
作者单位:[1]南华大学药物药理研究所,湖南省衡阳市421001 [2]湖南环境生物职业技术学院,湖南省衡阳市421005
基金项目:国家自然科学基金项目(30901577); 教育部留学回国人员科研启动基金(20091590)
摘    要:背景:结合课题组以往研究成果,提出caveolae可能参与apelin-13促血管平滑肌细胞增殖的假设。目的:实验观察细胞膜特殊凹陷结构caveolae参与G蛋白偶联受体APJ的内源性配体apelin-13促进大鼠血管平滑肌细胞增殖的作用。方法:采用组织贴块法培养大鼠胸主动脉血管平滑肌细胞,用MTT方法观察血管平滑肌细胞增殖,Western Blotting方法观察信号蛋白表达,免疫共沉淀技术检测信号分子复合物的形成。结果与结论:①caveolae结构破坏剂β-环糊精(5mmol/L,25h)可明显增强apelin-13诱导的血管平滑肌细胞增殖。②apelin-13(0,1,2,4,8μmol/L)刺激血管平滑肌细胞,caveolin-1的表达下调,在1μmol/L时下调明显。③β-环糊精(5mmol/L)破坏caveolae后,可使apelin-13下调caveolin-1表达的作用增强。④对照组(体积分数为0.1%胎牛血清孵育)及处理组(apelin-13刺激)caveolin-1与PI3K及ERK1/2均有复合物形成,在apelin-13刺激的情况caveolin-1-PI3K复合物减少、caveolin-1-ERK1/2复合物减少,即apelin-13可能促进caveolin-1与PI3K及ERK1/2解离。结果提示细胞膜特殊凹陷结构caveolae参与apelin-13促血管平滑肌细胞增殖作用。

关 键 词:血管平滑肌细胞  apelin-13  APJ  caveolae  caveolin-1  β-环糊精  PI3K  ERK1/2

apelin-13 promotes proliferation of vascular smooth muscle cells by downregulating caveolae expression
Mao Xiao-huan,Li Lan-fang,Gao Jing,Yang Li,Liu Wei,Qin Xu-ping,Chen Lin-xi.apelin-13 promotes proliferation of vascular smooth muscle cells by downregulating caveolae expression[J].Chinese Journal of Clinical Rehabilitation,2011(46):8603-8608.
Authors:Mao Xiao-huan  Li Lan-fang  Gao Jing  Yang Li  Liu Wei  Qin Xu-ping  Chen Lin-xi
Institution:1Institute of Pharmacy and Pharmacology,University of South China,Hengyang 421001,Hunan Province,China;2Hunan Polytechnic College of Environment and Biology,Hengyang 421005,Hunan Province,China
Abstract:BACKGROUND:Previous results have shown that caveolae is likely to participate in apelin-13 promotion of vascular smooth muscle cell proliferation.OBJECTIVE:APJ is a G-protein coupled receptor,and its ligand is apelin peptide.Previously,we reported PI3K and ERK1/2 signal pathway mediated proliferation of vascular smooth muscle cells(VSMCs) induced by apelin-13.This study is to observe caveolae involved in rat VSMCs proliferation induced by apelin-13 and to determine whether caveolin-1 protein binds to signal molecules PI3K,ERK1/2 to mediate VSMC proliferation induced by apelin-13.METHODS:VSMCs were prepared from male Sprague-Dawley rat thoracic aorta by the primary-explant method.The effect of β-cyclodextrin on cell proliferation induced by apelin-13 was measured by MTT assay.VSMCs were incubated with apelin-13 and β-cyclodextrin(β-CD) ,caveolin-1 expression was detected by western blot assay.Formation of high molecular weight polyprotein component including caveolin-1 and PI3K /ERK1/2 was detected by immunoprecipitation.RESULTS AND CONCLUSION:β-CD(5 mmol/L,25 hours) significantly enhanced VSMCs proliferation induced by apelin-13(P〈0.05) .Treating VSMCs with apelin-13(0,1,2,4,8 μmol/L) downregulated apelin-13-induced expression of caveolin-1 and the effect was distinct at 1μmol/L(P〈0.05) .Pretreatment of the cells with 5 mmol/L β-CD could strength the downregulation of apelin-13-induced caveolin-1 expression(P〈0.05) .Apelin-13 may induce dissociation of PI3K(ERK1/2) with caveolin-1 in VSMCs compared with the control group.These findings suggest that caveolae is involved in apelin-13-induced VSMCs proliferation.
Keywords:
本文献已被 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号